Deficiency of SPAG16L causes male infertility associated with impaired sperm motility
about
Targeted deletion of Tssk1 and 2 causes male infertility due to haploinsufficiency.Loss of SPEF2 function in mice results in spermatogenesis defects and primary ciliary dyskinesiaSam68 regulates translation of target mRNAs in male germ cells, necessary for mouse spermatogenesisMammalian axoneme central pair complex proteins: Broader roles revealed by gene knockout phenotypesMouse RC/BTB2, a member of the RCC1 superfamily, localizes to spermatid acrosomal vesiclesSperm-associated antigen 6 (SPAG6) deficiency and defects in ciliogenesis and cilia function: polarity, density, and beatSCO-ping out the mechanisms underlying the etiology of hydrocephalusAMP-activated kinase AMPK is expressed in boar spermatozoa and regulates motilitySperm-associated antigen-17 gene is essential for motile cilia function and neonatal survivalPrimary ciliary dyskinesia in mice lacking the novel ciliary protein Pcdp1.Functional deficiencies and a reduced response to calcium in the flagellum of mouse sperm lacking SPAG16LPhosphorylation of mouse sperm axoneme central apparatus protein SPAG16L by a testis-specific kinase, TSSK2Recombinant production of enzymatically active male contraceptive drug target hTSSK2 - Localization of the TSKS domain phosphorylated by TSSK2Germ cell-specific disruption of the Meig1 gene causes impaired spermiogenesis in mice.Intraflagellar transport protein IFT20 is essential for male fertility and spermiogenesis in miceThe hydrocephalus inducing gene product, Hydin, positions axonemal central pair microtubules.Expression, Localization of SUMO-1, and Analyses of Potential SUMOylated Proteins in Bubalus bubalis Spermatozoa.Transcription and post-transcriptional regulation of spermatogenesis.Spag16, an axonemal central apparatus gene, encodes a male germ cell nuclear speckle protein that regulates SPAG16 mRNA expression.Calcium channels in the development, maturation, and function of spermatozoa.Genetic variation in SPAG16 regions encoding the WD40 repeats is not associated with reduced sperm motility and axonemal defects in a population of infertile malesClinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome.A MEIG1/PACRG complex in the manchette is essential for building the sperm flagella.Transcriptional regulation of human sperm-associated antigen 16 gene by S-SOX5Mendelian genetics of male infertilityExpression profile of male germ cell-associated genes in mouse embryonic stem cell cultures treated with all-trans retinoic acid and testosteroneEnhanced response to pulmonary Streptococcus pneumoniae infection is associated with primary ciliary dyskinesia in mice lacking Pcdp1 and Spef2.Sperm flagella: comparative and phylogenetic perspectives of protein components.Riding the wave of ependymal cilia: genetic susceptibility to hydrocephalus in primary ciliary dyskinesia.A mutation study of sperm head shape and motility in the mouse: lessons for the clinic.The mouse transcription factor-like 5 gene encodes a protein localized in the manchette and centriole of the elongating spermatid.Proteomics analysis of adult testis from Bombyx mori.Gonadal transcriptomic analysis of yellow catfish (Pelteobagrus fulvidraco): identification of sex-related genes and genetic markers.The Central Apparatus of Cilia and Eukaryotic Flagella.Fused (Stk36) is a ciliary protein required for central pair assembly and motile cilia orientation in the mammalian oviduct.Biallelic Mutations in CFAP43 and CFAP44 Cause Male Infertility with Multiple Morphological Abnormalities of the Sperm Flagella.IFT25, an intraflagellar transporter protein dispensable for ciliogenesis in somatic cells, is essential for sperm flagella formation.Intraflagellar Transporter Protein 140 (IFT140), a component of IFT-A complex, is Essential for Male Fertility and Spermiogenesis in Mice.Sperm dysfunction and ciliopathy.Physcomitrella MADS-box genes regulate water supply and sperm movement for fertilization.
P2860
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P2860
Deficiency of SPAG16L causes male infertility associated with impaired sperm motility
description
2006 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2006
@ast
im Dezember 2005 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2006/04/01)
@sk
vědecký článek publikovaný v roce 2006
@cs
wetenschappelijk artikel (gepubliceerd op 2006/04/01)
@nl
наукова стаття, опублікована у квітні 2006
@uk
مقالة علمية (نشرت في أبريل 2006)
@ar
name
Deficiency of SPAG16L causes male infertility associated with impaired sperm motility
@ast
Deficiency of SPAG16L causes male infertility associated with impaired sperm motility
@en
Deficiency of SPAG16L causes male infertility associated with impaired sperm motility
@nl
type
label
Deficiency of SPAG16L causes male infertility associated with impaired sperm motility
@ast
Deficiency of SPAG16L causes male infertility associated with impaired sperm motility
@en
Deficiency of SPAG16L causes male infertility associated with impaired sperm motility
@nl
prefLabel
Deficiency of SPAG16L causes male infertility associated with impaired sperm motility
@ast
Deficiency of SPAG16L causes male infertility associated with impaired sperm motility
@en
Deficiency of SPAG16L causes male infertility associated with impaired sperm motility
@nl
P2093
P2860
P1476
Deficiency of SPAG16L causes male infertility associated with impaired sperm motility
@en
P2093
Aatish M Patel
Glenn L Radice
Igor Kostetskii
Jean Bennett
Jerome F Strauss
Lisa Haig-Ladewig
Rossana Sapiro
Stuart B Moss
Waixing Tang
Zhangyong Wei
P2860
P304
P356
10.1095/BIOLREPROD.105.049254
P407
P577
2005-12-28T00:00:00Z